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通过临床标本间接免疫荧光试验快速诊断拟杆菌感染。

Rapid diagnosis of Bacteroides infections by indirect immunofluorescence assay of clinical specimens.

作者信息

Kasper D L, Fiddian A P, Tabaqchali S

出版信息

Lancet. 1979 Feb 3;1(8110):239-42. doi: 10.1016/s0140-6736(79)90768-2.

Abstract

43 specimens from a variety of sites were directly examined by indirect immunofluorescence assay (I.F.A.) with specific antisera against the capsular polysaccharide of Bacteroides fragilis and pooled antisera against a number of serotypes of Bacteroides sp. (all of the former B. fragilis subspecies). The findings were compared with those of routine anaerobic bacteriology and gas liquid chromatography for short chain fatty acids. Examination by I.F.A. was a sensitive (100%) and specific (90.3%) means of identifying B. fragilis. Use of the pooled serum was sensitive (100%) but less specific (64.3%) than the capsular antiserum (90.3%) although it had the advantage of detecting Bacteroides species other than B. fragilis. The capsular serum I.F.A. gave 9.7% false positives and no false negatives. The predictive value of a positive identification of B. fragilis in a clinical specimen using this anticapsular serum I.F.A. test was 80%; with the pooled Bacteroides group-serum it was 60%. The predictive value of a negative test was 100% for both sera, indicating that a negative I.F.A. test is a reliable index of the absence of Bacteroides from the culture I.F.A. of clinical material provides a rapid (less than 2 h) specific and sensitive means for the diagnosis of B. fragilis infections and would be of use in a clinical laboratory.

摘要

采用针对脆弱拟杆菌荚膜多糖的特异性抗血清以及针对多种拟杆菌血清型(均为以前的脆弱拟杆菌亚种)的混合抗血清,通过间接免疫荧光试验(I.F.A.)对来自各种部位的43份标本进行直接检测。将这些结果与常规厌氧细菌学以及短链脂肪酸气液色谱分析的结果进行比较。通过I.F.A.检测是鉴定脆弱拟杆菌的一种敏感(100%)且特异(90.3%)的方法。使用混合血清虽然有检测除脆弱拟杆菌之外的其他拟杆菌属菌种的优势,但其敏感性为100%,但特异性(64.3%)低于荚膜抗血清(90.3%)。荚膜血清I.F.A.产生9.7%的假阳性,无假阴性。使用这种抗荚膜血清I.F.A.检测法对临床标本中脆弱拟杆菌阳性鉴定的预测值为80%;使用混合拟杆菌属群血清时为60%。两种血清的阴性检测预测值均为100%,这表明I.F.A.阴性检测是培养物中不存在拟杆菌的可靠指标。临床材料的I.F.A.检测提供了一种快速(少于2小时)、特异且敏感的方法用于诊断脆弱拟杆菌感染,在临床实验室中会很有用。

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